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| Study ID | Variant ID | Variant Region type | Variant Call type | Sampleset ID | Method | Analysis ID | Validation | Variant samples | Subject phenotype | Clinical Interpretation | Assembly | Accession | Chr | Outer-Start | Start | Inner-Start | Inner-End | End | Outer-End | Placement Type | Remap Score |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| nstd178 | nssv15768603 | copy number loss | Oligo aCGH | Curated | No | 176.30 | GRCh37 (hg19) | NC_000016.9 | 16 | 86542131 | 86549266 | Submitted genomic | |||||||||
| nstd178 | nssv15768603 | copy number loss | Oligo aCGH | Curated | No | 176.30 | GRCh37 (hg19) | NC_000016.9 | 16 | 86542131 | 86549266 | Submitted genomic | |||||||||
| nstd178 | nssv15768603 | copy number loss | Oligo aCGH | Curated | No | 176.30 | GRCh38.p12 | NC_000016.10 | 16 | 86508525 | 86515660 | Remapped | 1 | ||||||||
| nstd178 | nsv4449727 | copy number variation | No | GRCh37 (hg19) | NC_000016.9 | 16 | 86542131 | 86549266 | Submitted genomic | ||||||||||||
| nstd178 | nsv4449727 | copy number variation | No | GRCh37 (hg19) | NC_000016.9 | 16 | 86542131 | 86549266 | Submitted genomic | ||||||||||||
| nstd178 | nsv4449727 | copy number variation | No | GRCh38.p12 | NC_000016.10 | 16 | 86508525 | 86515660 | Remapped | 1 |